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  NF-κB is required for cell death induction by latent membrane protein 1 of Epstein-Barr virus

Nitta, T., Chiba, A., Yamashita, A., Rowe, M., Israël, A., Reth, M., et al. (2003). NF-κB is required for cell death induction by latent membrane protein 1 of Epstein-Barr virus. Cellular Signalling, 15(4), 423-433.

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 Creators:
Nitta, Takeshi, Author
Chiba, Ayako, Author
Yamashita, Atsuya, Author
Rowe, Martin, Author
Israël, Alain, Author
Reth, Michael1, Author           
Yamamoto, Naoki, Author
Yamaoka, Shoji, Author
Affiliations:
1Research Group and Chair of Molecular Immunology of the University of Freiburg, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243645              

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Free keywords: LMP1; NF-κB; apoptosis; cell death; caspase
 Abstract: NF-κB is a transcription factor known to promote or antagonize cell death depending on cell types and stimuli. Here, we demonstrate that expression of latent membrane protein 1 (LMP1), an Epstein-Barr virus (EBV)-encoded membrane protein, triggers programmed cell death in an NF-κB-dependent manner. Co-expression of NF-κB inhibitors completely prevented activation of NF-κB and LMP1-induced cell death. Addition therein of RelA, an active subunit of NF-κB, restored the NF-κB activation and cell death induction by LMP1, but RelA alone did not induce cell death. These results indicate that the activation of NF-κB is required for cell death induced by LMP1. Moreover, LMP1 induced activation of caspase-3 via the activation of NF-κB. Studies with z-VAD- fmk, a caspase inhibitor, indicated that NF-κB mediated both caspase-dependent and -independent death pathways. In conclusion, the cell death induced by LMP1 uncovered caspase- dependent and -independent death pathways both of which require NF-κB.

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Language(s): eng - English
 Dates: 2003-04
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 20956
ISI: 000181517500009
 Degree: -

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Title: Cellular Signalling
  Alternative Title : Cell. Signal.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 15 (4) Sequence Number: - Start / End Page: 423 - 433 Identifier: ISSN: 0898-6568